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Clinical Evaluation of i-STAT Analyzer Glucose, Hematocrit and Sodium for Capillary Samples

NCT02897154 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 297

Last updated 2018-03-20

No results posted yet for this study

Summary

The objective of this study is to compare the performance of two i-STAT Analyzers in a Point-of-Care (POC) setting. The evaluation will be performed using a cartridge to test glucose, hematocrit and sodium on capillary specimens.

Conditions

  • Analytical Performance of Sodium, Glucose and Hematocrit Assays by the i-STAT 500 (Alinity) Analyzer

Interventions

DIAGNOSTIC_TEST

In-vitro

Sponsors & Collaborators

  • Abbott Point of Care

    lead INDUSTRY

Principal Investigators

  • Chris P Edwards, BSc · Abbott Point of Care

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2016-05-10
Primary Completion
2017-03-15
Completion
2017-03-15

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02897154 on ClinicalTrials.gov